HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169167Generated: November 1, 2026
Thionyl Chloride → 4-chloro-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/1169167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(2-Chlorophenyl)propanoic acid | HCID 95676 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 4-chloro-2,3-dihydro-1H-inden-1-one | HCID 11332681 | 96.2% |
Reaction Steps
33.5 g (181 mmol) of the 1-(2-carboxyethyl)-2-chlorobenzene and 83.4 ml of thionyl chloride are placed in a reaction vessel and stirred at 80° C. for one hour. The excess thionyl chloride is subsequently taken off and the residue is admixed with 200 ml of heptane. The reaction mixture is stirred for 30 minutes and the solvent is subsequently removed in an oil pump vacuum. The residue is taken up in 536 ml of methylene chloride and, while cooling in ice, 48.4 g (363 mmol) of aluminum trichloride are added a little at a time over a period of 10 minutes. The resulting reaction solution is stirred at 0° C. for another 2 hours before the reaction mixture is poured onto 300 ml of ice water. After the aqueous phase has been separated off and extracted once with 60 ml of toluene, the combined organic phases are washed with 80 ml of water and with 100 ml of saturated NaCl solution. After drying over magnesium sulfate, the solvent is removed in an oil pump vacuum. 29 g (96%) of the desired product are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627764B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-22c45a0048a14569a1afb2f9294c9f15 |
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| Source note | uspto-grants-2003_09 |
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